Final outcome results of the multicenter isradipine diuretic atherosclerosis study (MIDAS) - A randomized controlled trial

被引:388
作者
Borhani, NO
Mercuri, M
Borhani, PA
Buckalew, VM
CanossaTerris, M
Carr, AA
Kappagoda, T
Rocco, MV
Schnaper, HW
Sowers, JR
Bond, MG
机构
[1] BOWMAN GRAY SCH MED,NEPHROL SECT,DEPT INTERNAL MED,WINSTON SALEM,NC 27157
[2] UNIV CALIF DAVIS,SCH MED,DIV CARDIOVASC MED,DAVIS,CA 95616
[3] UNIV CALIF DAVIS,SCH MED,DEPT INTERNAL MED,DAVIS,CA 95616
[4] UNIV NEVADA,SCH MED,DEPT FAMILY & COMMUNITY MED,RENO,NV 89557
[5] BOWMAN GRAY SCH MED,DIV VASC ULTRASOUND RES,WINSTON SALEM,NC 27157
[6] HEART RES INST,CLIN TRIALS UNIT,MIAMI,FL
[7] CIRCULATORY DIS CTR,AUGUSTA,GA
[8] SCI APPLICAT CO INC,BIRMINGHAM,AL
[9] PREVENT CARDIOL INC,BIRMINGHAM,AL
[10] WAYNE STATE UNIV,DIV ENDOCRINOL METAB & HYPERTENS,DETROIT,MI
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 1996年 / 276卷 / 10期
关键词
D O I
10.1001/jama.276.10.785
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective.-To compare the rate of progression of mean maximum intimal-medial thickness (IMT) in carotid arteries, using quantitative B-mode ultrasound imaging, during antihypertensive therapy with isradipine vs hydrochlorothiazide. Design.-Randomized, double-blind, positive-controlled trial. Setting.-Nine medical center clinics. Population.-A total of 883 patients with baseline mean+/-SD systolic and diastolic blood pressure (SBP and DBP, respectively) of 149.7+/-16.6 and 96.5+/-5.1 mm Hg, age of 58.5+/-8.5 years, and maximum IMT of 1.17+/-0.20 mm. Interventions.-Twice daily doses of isradipine (2.5-5.0 mg) or hydrochlorothiazide (12.5-25 mg). Main Outcome Measure (Primary End Point).-Rate of progression of mean maximum IMT in 12 carotid focal points over 3 years. Results.-There was no difference in the rate of progression of mean maximum IMT between isradipine and hydrochlorothiazide over 3 years (P=.68). There was a higher incidence of major vascular events (eg, myocardial infarction, stroke, congestive heart failure, angina, and sudden death) in isradipine (n=25; 5.65%) vs hydrochlorothiazide (n=14; 3.17%) (P=.07), and a significant increase in nonmajor vascular events and procedures (eg, transient ischemic attack, dysrhythmia, aortic valve replacement, and femoral popliteal bypass graft) in isradipine (n=40; 9.05%) vs hydrochlorothiazide (n=23; 5.22%) (P=.02). At 6 months, mean DBP decreased by 13.0 mm Hg in both groups, and mean SEP decreased by 19.5 mm Hg in hydrochlorothiazide and 16.0 mm Hg in isradipine (P=.002); the difference in SBP between the 2 groups persisted throughout the study but did not explain the increased incidence of vascular events in patients treated with isradipine. Conclusion.-The rate of progression of mean maximum IMT in carotid arteries, the surrogate end point in this study, did not differ between the 2 treatment groups. The increased incidence of vascular events in patients receiving isradipine compared with hydrochlorothiazide is of concern and should be studied further.
引用
收藏
页码:785 / 791
页数:7
相关论文
共 39 条
  • [1] MIDAS, THE MULTICENTER ISRADIPINE DIURETIC ATHEROSCLEROSIS STUDY - DESIGN-FEATURES AND BASE-LINE DATA
    APPLEGATE, WB
    BYINGTON, RP
    [J]. AMERICAN JOURNAL OF HYPERTENSION, 1991, 4 (02) : S114 - S117
  • [2] BOND MG, 1989, AM J MED, V86, P33
  • [3] BOND MG, 1991, J CARDIOVASC PHAR S4, V17, P87
  • [4] BORHANI NO, 1992, J CARDIOVASC PHAR S3, V19, P16
  • [5] BORHANI NO, 1991, J CARDIOVASC PHAR S3, V18, P15
  • [6] 1989 CORCORAN LECTURE - ADAPTIVE AND MALADAPTIVE RESPONSES OF THE ARTERIAL-WALL TO HYPERTENSION
    CHOBANIAN, AV
    [J]. HYPERTENSION, 1990, 15 (06) : 666 - 674
  • [7] CHOBANIAN AV, 1987, J HYPERTENS S4, V5, P43
  • [8] BLOOD-PRESSURE, STROKE, AND CORONARY HEART-DISEASE .2. SHORT-TERM REDUCTIONS IN BLOOD-PRESSURE - OVERVIEW OF RANDOMIZED DRUG TRIALS IN THEIR EPIDEMIOLOGIC CONTEXT
    COLLINS, R
    PETO, R
    MACMAHON, S
    HEBERT, P
    FIEBACH, NH
    EBERLEIN, KA
    GODWIN, J
    QIZILBASH, N
    TAYLOR, JO
    HENNEKENS, CH
    [J]. LANCET, 1990, 335 (8693) : 827 - 838
  • [9] CUTLER JA, 1989, HYPERTENSION S1, V13, P36
  • [10] Dahlof B, 1993, Blood Press, V2, P136, DOI 10.3109/08037059309077541